Incisive, Inc. (Formerly Named Incisive, LLC) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Incisive, Inc. (Formerly Named Incisive, LLC) - FDA 510(k) Cleared De...
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Cleared
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Denied
Incisive, Inc. (Formerly Named Incisive, LLC) has 1 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Incisive, Inc. (Formerly Named Incisive, LLC) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Incisive, Inc. (Formerly Named Incisive, LLC)
1 devices